Canonical Allele Identifier: CA286402663

Gene: GALNS

Linked Data

• ClinVar Variation Id: 1288302
• ClinVar RCV Id: RCV001707277
• dbSNP Id: rs79939637
• gnomAD v2: 16-88901998-C-T
• gnomAD v3: 16-88835590-C-T
• gnomAD v4: 16-88835590-C-T
• MyVariant Identifiers: chr16:g.88901998C>T (hg19) ; chr16:g.88835590C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88835590C>T , CM000678.2:g.88835590C>T	GRCh38
NC_000016.9:g.88901998C>T , CM000678.1:g.88901998C>T	GRCh37
NC_000016.8:g.87429499C>T	NCBI36
NG_008667.1:g.26377G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.758+135G>A MANE Select	ENSP00000268695.5:n.758+135G>A
ENST00000268695.9:c.758+135G>A	ENSP00000268695.5:n.758+135G>A
ENST00000562593.5:n.4167+135G>A
ENST00000562931.5:n.346+135G>A
ENST00000567525.5:c.439+135G>A	ENSP00000454484.1:n.439+135G>A
ENST00000568613.5:c.877+135G>A	ENSP00000457921.1:n.877+135G>A
NM_000512.4:c.758+135G>A	NP_000503.1:n.758+135G>A
XM_005256301.2:c.758+135G>A	XP_005256358.1:n.758+135G>A
XM_005256302.1:c.776+135G>A	XP_005256359.1:n.776+135G>A
XM_011522982.1:c.776+135G>A	XP_011521284.1:n.776+135G>A
XM_011522984.1:c.776+135G>A	XP_011521286.1:n.776+135G>A
NM_001323543.1:c.203+135G>A	NP_001310472.1:n.203+135G>A
NM_001323544.1:c.776+135G>A	NP_001310473.1:n.776+135G>A
XM_005256301.3:c.758+135G>A	XP_005256358.1:n.758+135G>A
XM_011522982.2:c.776+135G>A	XP_011521284.1:n.776+135G>A
XM_017023111.2:c.776+135G>A	XP_016878600.1:n.776+135G>A
XM_017023112.2:c.776+135G>A	XP_016878601.1:n.776+135G>A
XM_017023113.1:c.203+135G>A	XP_016878602.1:n.203+135G>A
NM_000512.5:c.758+135G>A MANE Select	NP_000503.1:n.758+135G>A
NM_001323543.2:c.203+135G>A	NP_001310472.1:n.203+135G>A
NM_001323544.2:c.776+135G>A	NP_001310473.1:n.776+135G>A